A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2722915



Internal ID10306551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63365894..63366454hg38UCSC Ensembl
Outerchr20:61997246..61997806hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6873875, essv6877373, essv6925264, essv6846647, essv6941367, essv6780419, essv6666077, essv6710293
SamplesSSM011, SSM041, SSM092, SSM018, SSM067, SSM085, SSM022, SSM004
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2722915
Frequency
Sample Size96
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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